Theodor Boveri Institute, Department of Biochemistry and Molecular Biology, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany; Mildred Scheel Early Career Center, University Hospital Würzburg, Würzburg, Germany.
Theodor Boveri Institute, Department of Biochemistry and Molecular Biology, Biocenter, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.
Trends Cancer. 2023 Oct;9(10):805-816. doi: 10.1016/j.trecan.2023.06.008. Epub 2023 Jul 7.
MYC oncoproteins are key drivers of tumorigenesis. As transcription factors, MYC proteins regulate transcription by all three nuclear polymerases and gene expression. Accumulating evidence shows that MYC proteins are also crucial for enhancing the stress resilience of transcription. MYC proteins relieve torsional stress caused by active transcription, prevent collisions between the transcription and replication machineries, resolve R-loops, and repair DNA damage by participating in a range of protein complexes and forming multimeric structures at sites of genomic instability. We review the key complexes and multimerization properties of MYC proteins that allow them to mitigate transcription-associated DNA damage, and propose that the oncogenic functions of MYC extend beyond the modulation of gene expression.
MYC 癌基因蛋白是肿瘤发生的关键驱动因素。作为转录因子,MYC 蛋白通过三种核聚合酶调节转录和基因表达。越来越多的证据表明,MYC 蛋白对于增强转录的应激弹性也至关重要。MYC 蛋白通过参与一系列蛋白质复合物并在基因组不稳定部位形成多聚体结构,缓解活性转录引起的扭转应力,防止转录和复制机制之间的碰撞,解决 R 环,并通过修复 DNA 损伤来缓解转录引起的 DNA 损伤。我们回顾了允许 MYC 蛋白减轻与转录相关的 DNA 损伤的关键复合物和多聚化特性,并提出 MYC 的致癌功能超出了对基因表达的调节。